Process to prepare a surface-reacted calcium carbonate implementing a weak acid, resulting products and uses thereof

ABSTRACT

The present application relates to a process for preparing a surface-reacted calcium carbonate in an aqueous environment. The process according to the present invention aims at avoiding the mandatory implementation of medium-strong to strong acids. Another aspect of the present invention is directed to an aqueous suspension of surface-reacted calcium carbonate which is obtainable by the inventive process.

CROSS-REFERENCE TO RELATED APPLICATIONS

This is a divisional of U.S. application Ser. No. 13/378,171, filed Jan.17, 2012, which is a U.S. National phase of PCT Application No.PCT/IB2010/052666, filed Jun. 15, 2010, which claims priority toEuropean Application No. 09162727.3, filed Jun. 15, 2009 and U.S.Provisional Application No. 61/269,243, filed Jun. 22, 2009, thecontents of which are hereby incorporated by reference.

The present invention concerns the technical field of surface-reactedcalcium carbonate products based on ground natural calcium carbonate(GNCC).

In practice, calcium carbonate is used in large quantities in the paper,paint, rubber and plastics industries for various purposes such ascoatings, fillers, extenders and pigments for papermaking as well asaqueous lacquers and paints and in water treatment, and notably as ameans of removing inorganic materials such as heavy metals and/orpharmaceutical waste such as polycyclic compounds, cholesterol and/orendocrine disrupting compounds (EDC).

In the past decade, a new class of calcium carbonate derivativesreferred to as “surface-reacted calcium carbonate” has been developedand provides a number of advantageous properties on application.

A “surface-reacted calcium carbonate” is a material comprising calciumcarbonate and an insoluble, at least partially crystalline,non-carbonate calcium salt extending from the surface of at least partof the calcium carbonate. The calcium ions forming said at leastpartially crystalline non-carbonate calcium salt originate largely fromthe starting calcium carbonate material that also serves to form thesurface-reacted calcium carbonate core.

In the art, several approaches for preparing such surface-reactedcalcium carbonate products have been proposed.

U.S. Pat. No. 6,666,953 B1 relates to a pigment, filler or mineralcontaining a natural calcium carbonate, treated with one or moreproviders of H₃O⁺ ions having a pKa of less than 2.5 and gaseous CO₂,allowing a reduction in the weight of paper for a constant surface areawithout loss of physical properties when it is used as a pigment orcoating filler for said paper.

Variant WO 2005/121257 A2 discloses a method for producing a dry mineralpigment characterised in that it contains a product formed in situ bythe multiple reaction of a calcium carbonate with a medium-strong tostrong acid and with gaseous CO₂ formed in situ and/or from an externalsupply, along with at least one compound of formula R-X.

Likewise, WO 2004/083316 A1 refers to mineral pigments containing aproduct formed in situ by the double and/or multiple reaction between acalcium carbonate and the reaction product or products of the saidcarbonate with one or more moderately strong to strong H₃O⁺ ion donorsand the reaction product or products of the said carbonate with gaseousCO₂ formed in situ and/or coming from an external supply, and at leastone aluminium silicate and/or at least one synthetic silica and/or atleast one calcium silicate and/or at least one silicate of a monovalentsalt such as sodium silicate and/or potassium silicate and/or lithiumsilicate, preferably such as sodium silicate and/or at least onealuminium hydroxide and/or at least one sodium and/or potassiumaluminate, used in papermaking applications, such as mass filling and/orpaper coating.

The above technologies are of particular interest to the skilled man asthey provide a means of structuring the surface and significantlyincreasing the specific surface area of the GNCC starting material bycontrolled deposition of an at least partially crystalline calcium saltthereon, and such that the calcium source for this deposited material isthe GNCC mineral itself.

However, each involves the use of medium-strong to strong acidscharacterised by a pKa of less than 2.5 when measured at 20° C. Many ofthe acids listed as useful medium-strong to strong acids are mineralacids, and preferred acids include notably phosphoric acid.

Firstly, the skilled man remains constantly interested in new processesto prepare surface-reacted calcium carbonate materials implementingalternative adducts, given that the availability and price of a givenadduct are subject to change over time, including unexpected changesthat the skilled man must plan for.

Secondly, with regards the occupational exposure limits established by acooperation between the International Programme on Chemical Safety andthe European Commission, and notably according to the InternationalChemical Safety Card (ICSC) of phosphoric acid published by theInternational Occupational Safety and Health Information Centre (CIS),this acid is associated with a very low threshold limit value (TLV)corresponding to less than 1 ppm as a time weighted average (TWA). Thisimplies that particular and often onerous precautions are to be takenwhen implementing this acid, notably on the industrial scale. Theskilled man is moreover aware of the risk that regulations covering suchlow TLV substance become more stringent over time, potentially renderingtheir employment impracticable.

Faced with the above, the Applicant has surprisingly found a process toprepare a surface-reacted calcium carbonate having comparable specificsurface area development potential to surface-reacted calcium carbonateprepared according to U.S. Pat. No. 6,666,953 B1, but avoiding themandatory implementation of medium-strong to strong acids such asphosphoric acid.

This inventive process resides in a particular, unexpected selection ofadducts, dosed according to a specific order of steps.

Namely, this process for preparing a surface-reacted calcium carbonatein an aqueous environment comprises the following steps:

a) providing at least one ground natural calcium carbonate (GNCC);b) providing at least one water-soluble acid;c) providing gaseous CO₂;d) contacting said GNCC of step a) with said acid of step b) and withsaid CO₂ of step c);characterised in that:

-   -   (i) said acid(s) of step b) each having a pK_(a) of greater than        2.5 and less than or equal to 7, when measured at 20° C.,        associated with the ionisation of their first available        hydrogen, and a corresponding anion formed on loss of this first        available hydrogen capable of forming water-soluble calcium        salts;    -   (ii) following contacting said acid(s) with said GNCC, at least        one water-soluble salt, which in the case of a        hydrogen-containing salt has a pK_(a) of greater than 7, when        measured at 20° C., associated with the ionisation of the first        available hydrogen, and the salt anion of which is capable of        forming water-insoluble calcium salts, is additionally provided.

When the prior art makes reference to contacting calcium carbonate witha weak acid, it is in view of an entirely different goal and accordingto processes that differ fundamentally from the process of the presentinvention.

Notably, U.S. Pat. No. 5,584,923, U.S. Pat. No. 5,647,902, U.S. Pat. No.5,711,799, WO 97/08247 A1 and WO 98/20079 A1, respectively, describecalcium carbonates which are made acid-resistant to enable their use asa filler material in the making of neutral to weakly acidic paper, and aprocess for producing such acid-resistant calcium carbonates. TheApplicant would point out that acid resistance is entirely incontradiction to the goal of the present invention, wherein the processimplements acid to act upon and liberate calcium ions from GNCC, whichthereafter serve in the development of surface area.

U.S. Pat. No. 5,043,017 likewise relates to calcium carbonate,acid-stabilized by the addition of one of a calcium-chelating agent anda conjugate base, such as sodium hexametaphosphate, followed by theaddition of an acid, which may be a weak acid. Not only does thisdocument refer, as above, to the goal of forming acid-resistant calciumcarbonate, but moreover underlines the importance of feeding thecalcium-chelating agent or conjugate base to the calcium carbonatebefore the weak acid.

WO 99/02608 A1 describes a method of producing a high solids slurry ofan acid-resistant precipitated calcium carbonate, wherein a solidsslurry is treated with a chemical additive, such as sodium aluminate, inorder to impart acid resistance to the calcium carbonate.

For completeness, the Applicant would like to mention unpublishedEuropean patent application having filing number 07 123 077.5, whichrelates to a process to prepare a surface-reacted calcium carbonatebased on PCC.

The prior art thus seems to be silent on economic methods for preparinghigh surface area surface-reacted calcium carbonate materials based onGNCC while avoiding the implementation of medium-strong to strong acidshaving a pK_(a) of less than 2.5 as measured at 20° C., such asphosphoric acid.

The present invention aims at providing such a process for preparingsurface-reacted calcium carbonate as described in the presentApplication and defined in the claims.

Accordingly, one object of the present application is a process forpreparing a surface-reacted calcium carbonate in an aqueous environmentcomprising the following steps:

a) providing at least one ground natural calcium carbonate (GNCC);b) providing at least one water-soluble acid;c) providing gaseous CO₂;d) contacting said GNCC of step a) with said acid of step b) and withsaid CO₂ of step c);characterised in that:

-   -   (i) said acid(s) of step b) each having a pK_(a) of greater than        2.5 and less than or equal to 7, when measured at 20° C.,        associated with the ionisation of their first available        hydrogen, and a corresponding anion formed on loss of this first        available hydrogen capable of forming water-soluble calcium        salts;    -   (ii) following contacting said acid(s) with said GNCC, at least        one water-soluble salt, which in the case of a        hydrogen-containing salt has a pK_(a) of greater than 7, when        measured at 20° C., associated with the ionisation of the first        available hydrogen, and the salt anion of which is capable of        forming water-insoluble calcium salts, is additionally provided.

“Ground natural calcium carbonate” (GNCC) in the meaning of the presentinvention is a calcium carbonate obtained from natural sources, marble,chalk or limestone, and processed through a treatment such as grinding,with or without grinding aids, screening and/or fractionizing wet and/ordry, for example by a cyclone.

For the purpose of the present application, “water-insoluble” materialsare defined as materials which, when mixed with deionised water andfiltered on a filter having a 0.2 μm pore size at 20° C. to recover theliquid filtrate, provide less than or equal to 0.1 g of recovered solidmaterial following evaporation at 95 to 100° C. of 100 g of said liquidfiltrate. “Water-soluble” materials are defined as materials leading tothe recovery of greater than 0.1 g of recovered solid material followingevaporation at 95 to 100° C. of 100 g of said liquid filtrate.

An “acid” in the meaning of the present invention is defined as aBronsted-Lowry acid, that is to say, it is an H₃O⁺ ion-provider. An“acid salt” is defined as a hydrogen-containing salt that is partiallyneutralised by an electropositive element other than hydrogen. A “salt”is defined as an electrically neutral ionic compound formed of anionsand cations.

For the purpose of the present application, pK_(a) is the symbolrepresenting the acid dissociation constant associated with a givenionisable hydrogen in a given acid, and is indicative of the naturaldegree of dissociation of this hydrogen from this acid at equilibrium inwater at a given temperature. Such pK_(a) values may be found inreference textbooks such as Harris, D.C. “Quantitative ChemicalAnalysis: 3^(rd) Edition”, 1991, W.H. Freeman & Co. (USA), ISBN0-7167-2170-8.

In accordance with the present invention, a “surface-reacted calciumcarbonate” is a material comprising calcium carbonate and an insoluble,at least partially crystalline, calcium salt of one or more anions ofsaid water-soluble salt under (ii) above. In a preferred embodiment, theinsoluble calcium salt extends from the surface of at least part of thecalcium carbonate. The calcium ions forming said at least partiallycrystalline calcium salt of said anion originate largely from thestarting calcium carbonate material. Such salts may include OH− anionsand/or crystal water.

Preferred Embodiments Relative to Step a)

In step a) of the process of the present invention, at least one groundnatural calcium carbonate (GNCC) is provided.

Preferably, said GNCC is selected from the group consisting of marble,chalk, calcite, dolomite, limestone and mixtures thereof.

In a preferred embodiment, said GNCC of step a) has a weight mediandiameter of 0.01 to 10 μm, and more preferably of 0.5 to 2 μm, asmeasured according to the measurement method provided in the Examplessection here below.

In another preferred embodiment, GNCC is provided in the form of anaqueous GNCC suspension.

In this preferred embodiment, said suspension has a pH of less than 11,and more preferably of less than 10.5, as measured according to themeasurement method described in the Examples section here below.

Preferably, the aqueous calcium carbonate suspension has a solidscontent of greater than or equal to 10 wt.-% and more preferably ofbetween 10 wt.-% and 80 wt.-%, based on the weight of the suspension.The applicant would remark that in the case of very high solidscontents, it is a requirement to have sufficient water for the reactionsduring and subsequent to step d) to occur. More preferably, the aqueouscalcium carbonate suspension has a solid content in the range of 16wt.-% to 60 wt.-%, and even more preferably in the range of 16 wt.-% to40 wt.-%, based on the weight of the suspension.

The suspension may moreover be stabilized by the addition ofdispersants. Conventional dispersants known to the skilled person can beused. The dispersant can be anionic, cationic or non-ionic. A preferreddispersant is polyacrylic acid.

Preferred Embodiments Relative to Step b)

Step b) of the process of the present invention refers to providing atleast one water-soluble acid. Said acid(s) each have a pK_(a) of greaterthan 2.5 and less than or equal to 7, when measured at 20° C.,associated with the ionisation of their first available hydrogen, and acorresponding anion formed on loss of this first available hydrogencapable of forming water-soluble calcium salts.

In a preferred embodiment, said water-soluble acid(s) have a pKa ofbetween 2.6 and 5.

In a more preferred embodiment, said water-soluble acid(s) are selectedfrom the group consisting of acetic acid, formic acid, propanoic acidand mixtures thereof. In an even more preferred embodiment, saidwater-soluble acid(s) are selected from the group consisting of aceticacid, formic acid and mixtures thereof. In a most preferred embodiment,said water-soluble acid is acetic acid.

Said water-soluble acid(s) of step b) are preferably dosed in a totalamount corresponding to at least 1.5×10⁻⁴ mol of hydrogen atoms in theacid/m² GNCC provided in step a), more preferably in a total amountcorrespond to from 2×10⁻⁴ to 12×10⁻⁴ mol of hydrogen atoms in theacid/m² GNCC provided in step a), and most preferably from 3×10⁻⁴ to10×10⁻⁴ mol of hydrogen atoms in the acid/m² GNCC provided in step a).

If the water-soluble salt contacted with said GNCC comprises one or morehydrogen atoms, the water-soluble acid of step b) may be dosed in alesser amount taking into account the equivalent mol hydrogen atoms ofthe salt—calculated assuming full dissociation of the hydrogen ion,regardless of actual pKa associated with the hydrogen atoms of the salt.In such a case the water-soluble acid will be dosed in an amount suchthat the total equivalent mols of hydrogen atoms, based on thewater-soluble acid and on the hydrogen-containing salt, corresponds toat least 1.5×10⁻⁴ mol of hydrogen atoms in the acid/m² GNCC provided instep a), more preferably in a total amount correspond to from 2×10 to12×10⁻⁴ mol of hydrogen atoms in the acid/m² GNCC provided in step a),and most preferably from 3×10⁻⁴ to 10×10⁻⁴ mol of hydrogen atoms in theacid/m² GNCC provided in step a).

Alternatively, said water-soluble acid(s) of step b) are preferablydosed in a total amount corresponding to 5 to 40 wt.-% equivalent pureacid based on the dry weight of GNCC provided in step a), morepreferably in a total amount corresponding to 10 to 30 wt.-% equivalentpure acid based on the dry weight of GNCC provided in step a), and mostpreferably in a total amount corresponding to 15 to 25 wt.-% equivalentpure acid based on the dry weight of GNCC provided in step a).

Said water-soluble acid(s) of step b) are preferably provided in theform of an aqueous solution having an acid concentration, determined asthe equivalent weight of pure acid on the weight of the total solution,corresponding to from 25 to 75%, and more preferably to from 40 to 60%.

Preferred Embodiments Relative to Step c)

According to step c) of the process of the present invention, gaseousCO₂ is provided.

The required carbon dioxide may be formed in situ from the carbonate asa result of contacting the acid with GNCC. Alternatively oradditionally, the carbon dioxide can be supplied from an externalsource.

Preferably, the concentration of gaseous carbon dioxide in the aqueoussuspension throughout the reaction is, in terms of volume, such that theratio (volume of suspension):(volume of gaseous CO₂) is from 1:0.05 to1:20, even more preferably 1:0.05 to 1:5.

Preferred Embodiments Relative to Step d)

Step d) of the process of the present invention refers to contactingsaid GNCC of step a) with said acid of step b) and with said CO₂ of stepc).

It is preferred that said acid(s) be added, in one or more steps, tosaid GNCC.

In the case where said GNCC is added to said acid(s), it is necessary toproceed adding a fraction of said GNCC to a fraction of said acid(s),and repeating this additional process until all of said GNCC has beencontacted with all of said acid(s).

Acid treatment and treatment with carbon dioxide can be carried outsimultaneously and automatically takes place when acid is used. It isalso possible to carry out an inventive acid treatment first, followedby treatment with carbon dioxide supplied from an external source.

Acid addition to GNCC may be performed dropwise or in one step. In thecase of dropwise addition, this addition preferably takes place within atime period of 10 minutes. It is more preferred to add said acid in onestep.

Preferred Embodiments Relative to Water-Soluble Salt

Following contacting said acid(s) of step b) with said GNCC of step a)during step d), at least one water-soluble salt, which in the case of ahydrogen-containing salt has a pK_(a) of greater than 7, when measuredat 20° C., associated with the ionisation of the first availablehydrogen, and the salt anion of which is capable of formingwater-insoluble calcium salts, is additionally provided.

The cation of said water-soluble salt is preferably selected from thegroup consisting of potassium, sodium, lithium and mixtures thereof. Ina more preferred embodiment, said cation is sodium. It is of note thatdepending on the charge of the anion, more than one of said cations maybe present to provide an electrically neutral ionic compound.

The anion of said water-soluble salt is preferably selected from thegroup consisting of phosphate, dihydrogen phosphate, monohydrogenphosphate, oxalate, silicate, mixtures thereof and hydrates thereof. Ina more preferred embodiment, said anion is selected from the groupconsisting of phosphate, dihydrogen phosphate, monohydrogen phosphate,mixtures thereof and hydrates thereof. In a most preferred embodiment,said anion is selected from the group consisting of dihydrogenphosphate, monohydrogen phosphate, mixtures thereof and hydratesthereof.

Said anion of said water-soluble salt(s) is preferably dosed in a totalamount corresponding to at least 5×10⁻⁵ mol of anion/m² GNCC provided instep a). More preferably, said anion of said water-soluble salt(s) isdosed in a total amount corresponding to 5×10⁻⁵ to 50×10⁻⁵ mol ofanion/m² GNCC provided in step a), and even more preferably in a totalamount corresponding to 10×10⁻⁵ to 30×10⁻⁵ mol of anion/m² GNCC providedin step a).

Water-soluble salt addition may be performed dropwise or in one step. Inthe case of dropwise addition, this addition preferably takes placewithin a time period of 10 minutes. It is more preferred to add saidsalt in one step.

Reaction Environment

Step d) and addition of said water-soluble salt preferably take place ina stirred reactor under stirring conditions such as to develop anessentially laminar flow.

Step d) and addition of said water-soluble salt preferably take place inan aqueous environment having a temperature of above 50° C., andpreferably of above 60° C.

Product Obtained from the Process

Subsequent to addition of said at least one water-soluble salt, the pHof the aqueous suspension, measured at 20° C., usually may reach a valueof greater than 6.0, preferably greater than 6.5, more preferablygreater than 7.0, even more preferably greater than 7.5. In other words,a surface-reacted calcium carbonate as an aqueous suspension having a pHof greater than 6.0, preferably greater than 6.5, more preferablygreater than 7.0, even more preferably greater than 7.5 is obtained. Ifthe aqueous suspension is allowed to reach equilibrium, the pH usuallyis greater than 7. A pH of greater than 6.0 may be adjusted without theaddition of a base when stirring of the aqueous suspension is continuedfor a sufficient time period, preferably 1 hour to 10 hours, morepreferably 1 to 5 hours.

Alternatively, prior to reaching an equilibrium state, which occurs at apH greater than 7, the pH of the aqueous suspension may be increased toa value greater than 6 by adding a base subsequent to carbon dioxidetreatment. Any conventional base such as sodium hydroxide or potassiumhydroxide can be used.

The obtained surface-reacted calcium carbonate suspension may beconcentrated, optionally up to the point of obtaining a drysurface-reacted calcium carbonate product. If the aqueous suspensiondescribed above is de-watered, the obtained solid (i.e. containingsufficiently little water so that it is not in a fluid form, or even nowater) surface-reacted calcium carbonate may be in the form of a cake,granules or a powder. This solid product may additionally be treatedwith fatty acids or other hydrophobising/oleophilising agents. Thissolid product may be washed with water.

Thus, a suspension of surface-reacted calcium carbonate is obtained,wherein said surface-reacted calcium carbonate comprises an insoluble,preferentially at least partially crystalline, calcium salt of anion(s)of said at least one water-soluble salt, which preferably extends fromthe surface of at least part of the calcium carbonate; provided in stepa).

In a preferred embodiment, the surface-reacted calcium carbonateobtained by the inventive process has a specific surface area of morethan 20 m²/g, e.g. 20 m²/g to 200 m²/g, more preferably more than 30m²/g, e.g. 30 m²/g to 150 m²/g and even more preferably more than 80m²/g, measured according to the measurement method provided in theExamples section below.

In a preferred embodiment, the surface-reacted calcium carbonate has aspecific BET surface area within the range of 20 to 150 m²/g or 30 to200 m²/g and a median grain diameter within the range of 0.1 to 50 μm.

Furthermore, it is preferred that the surface-reacted calcium carbonatehas a median grain diameter of from 0.1 to 50 μm, preferably of from 1to 25 μm, more preferably of from 3 to 15 μm, even more preferably offrom 5 to 12 μm as measured according to the measurement method providedin the Examples section below.

Preferably, the surface-reacted natural calcium carbonate has anintra-particle porosity within the range of 20% vol to 40% vol, measuredby mercury porosimetry. Intra-particle porosity by mercury porosimetryis determined according to the following protocol: tablets are made fromsuspensions of the surface-reacted natural calcium carbonate by applyinga constant pressure to the suspension for several hours such that wateris released by filtration through a fine 0.025 μm filter membraneresulting in a compacted tablet of the pigment. The tablets are removedfrom the apparatus and dried in an oven at 80° C. for 24 hours. Oncedried, single portions from each of the tablet blocks are characterisedby mercury porosimetry for porosity and pore size distribution using aMicromeritics Autopore IV mercury porosimeter. The maximum appliedpressure of mercury is 414 MPa, equivalent to a Laplace throat diameterof 0.004 μm (i.e. ˜nm). The mercury intrusion measurements are correctedfor the compression of mercury, expansion of the penetrometer andcompressibility of the solid phase of the sample. The intra-particlepores have to be distinguished from the inter-particle pores. For this,the tablet structure has to be confirmed as being discretely separablein pore size distribution, i.e. of essentially non-overlapping size,such that inter and intra-particle pore sizes are distinguishable.Further details of the measuring method are described in Transport inPorous Media (2006) 63: 239-259.

The inventive surface-reacted calcium carbonate or a slurry of saidsurface-reacted calcium carbonate may be used in paper, tissue paper,plastics, paints, or as a controlled release or water treatment agent.

The surface-reacted calcium carbonate obtained by the process of thepresent invention is preferably brought into contact with water to bepurified, e.g. industrial waste water, drinking water, urban wastewater, waste water from breweries, or water in the paper industry, byany conventional means known to the skilled person.

The surface-reacted calcium carbonate can be added as an aqueoussuspension, e.g. the suspension described above. Alternatively, it canbe added to the water to be purified in any appropriate solid form, e.g.in the form of granules or a powder or in the form of a cake.

The water may contain organic impurities, e.g. resulting from humanwaste, organic materials, soil, surfactants as well as inorganicimpurities, in particular heavy metal impurities such as iron- ormanganese-containing compounds. Harmful components that can be removedfrom the water with the purification process of the present inventionalso include microorganism such as bacteria, fungi, archaea, orprotists.

The following examples are meant to illustrate the invention withoutrestricting its scope.

EXAMPLES Measurement Methods

The following measurement methods are used to evaluate the parametersgiven in the examples and claims.

Specific Surface Area (SSA) of a Material

The specific surface area is measured via the BET method according toISO 9277 using nitrogen, following conditioning of the sample by heatingat 250° C. for a period of 30 minutes. Prior to such measurements, thesample is filtered, rinsed and dried at 90-100° C. in an oven for atleast 12 hours before being broken down in a mortar and pestle, and thenplaced in a mass balance at 130° C. until a constant weight is observed.

Particle Size Distribution (Mass % Particles with a Diameter <X) andWeight Median Grain Diameter (d₅₀) of Non-Surface Reacted CalciumCarbonate Particulate Material (Ie. GNCC)

Weight median grain diameter and grain diameter mass distribution of aparticulate material, such as GNCC, are determined via the sedimentationmethod, i.e. an analysis of sedimentation behaviour in a gravimetricfield. The measurement is made with a Sedigraph™ 5120.

The method and the instrument are known to the skilled person and arecommonly used to determine grain size of fillers and pigments. Themeasurement is carried out in an aqueous solution of 0.1 wt.-% Na₄P₂O₇.The samples were dispersed using a high speed stirrer and ultrasonic.

Median Grain Diameter (d₅₀) of Surface-Reacted Calcium Carbonate

Median grain diameter of surface-reacted calcium carbonate is determinedusing a Malvern Mastersizer 2000 Laser Diffraction System.

pH of an Aqueous Slurry

The pH of the aqueous suspension is measured using a standard pH-meterat approximately 25° C.

Solids Content of an Aqueous Slurry

The slurry solids content (also known as “dry weight”) is determinedusing a Moisture Analyser HR73 commercialised by Mettler-Toledo with thefollowing settings: temperature of 120° C., automatic switch off 3,standard drying, 5-20 g of slurry.

Example 1

The following Example is illustrative of the prior art, and involvescontacting GNCC with phosphoric acid.

A calcium carbonate suspension is prepared by adding water andundispersed chalk (having a d₅₀ of 1 μm, wherein 90% of particles have adiameter of less than 2 μm (Sedigraph)) to a 20-L stainless steelreactor, such that the aqueous suspension obtained has a solids contentcorresponding to 16% by dry weight relative to the total suspensionweight. The temperature of this suspension is thereafter brought to andmaintained at 70° C.

Under stirring at approximately 1000 rpm such that an essentiallylaminar flow is established, phosphoric acid in the form a 10% solutionis added to the calcium carbonate suspension through a peristaltic pumpover a period of 10 minute in an amount corresponding to 10% by weighton dry calcium carbonate weight and approximately 3×10⁻⁴ mol equivalenthydrogen/m² GNCC. Following this addition, CO₂ gas bubbles were observedto form and pass upwards through the suspension.

The suspension is stirred for an additional 5 minutes.

The resulting suspension is allowed to sit overnight. The product has anSSA=24.0 m²/g and a d₅₀=3.5 μm (Malvern).

Example 2

The following Example is illustrative of the prior art, and involvescontacting GNCC with phosphoric acid.

A calcium carbonate suspension is prepared by adding water andundispersed chalk (having a d₅₀ of 3 μm, wherein 33% of particles have adiameter of less than 2 μm (Sedigraph)) to a 100-L stainless steelreactor, such that the aqueous suspension obtained has a solids contentcorresponding to 16% by dry weight relative to the total suspensionweight. The temperature of this suspension is thereafter brought to andmaintained at 70° C.

Under stirring at approximately 1000 rpm such that an essentiallylaminar flow is established, phosphoric acid in the form a 30% solutionis added to the calcium carbonate suspension through a peristaltic pumpover a period of 10 minute in an amount corresponding to 25% by weighton dry calcium carbonate weight and approximately 2.6×10⁻⁴ molequivalent hydrogen/m² GNCC. Following this addition, CO₂ gas bubbleswere observed to form and pass upwards through the suspension.

The suspension is stirred for an additional 5 minutes.

The resulting suspension is allowed to sit overnight. The product has anSSA=34.5 m²/g and a d₅₀=7.9 μm (Malvern).

Example 3

The following Example is illustrative of the prior art, and involvescontacting GNCC with phosphoric acid.

A calcium carbonate suspension is prepared by adding water and dispersedmarble (having a d₅₀ of 0.7 μm, wherein 90% of particles have a diameterof less than 2 μm (Sedigraph)) in a 20-L stainless steel reactor, suchthat the aqueous suspension obtained has a solids content correspondingto 16% by dry weight relative to the total suspension weight. Thetemperature of this suspension is thereafter brought to and maintainedat 70° C.

Under stirring at approximately 1000 rpm such that an essentiallylaminar flow is established, phosphoric acid in the form a 10% solutionis added to the calcium carbonate suspension through a peristaltic pumpover a period of 10 minute in an amount corresponding to 30% by weighton dry calcium carbonate weight and approximately 9×10⁻⁴ mol equivalenthydrogen/m² GNCC. Following this addition, CO₂ gas bubbles were observedto form and pass upwards through the suspension.

The suspension is stirred for an additional 5 minutes.

The resulting suspension is allowed to sit overnight. The product has anSSA=35.0 m²/g and a d₅₀=3.9 μm (Malvern).

Example 4

The following Example is illustrative of the invention.

A calcium carbonate suspension is prepared by adding water andundispersed chalk (having a d₅₀ of 3 μm, wherein 33% of particles have adiameter of less than 2 μm

(Sedigraph)) in a 20-L stainless steel reactor, such that the aqueoussuspension obtained has a solids content corresponding to 16% by dryweight relative to the total suspension weight. The temperature of thissuspension is thereafter brought to and maintained at 70° C.

Under stirring at approximately 1000 rpm such that an essentiallylaminar flow is established, acetic acid in the form a 50% solution isadded to the calcium carbonate suspension through a separation funnelover a period of 1 minute in an amount corresponding to 18.4% by weighton dry calcium carbonate weight and 3×10⁻⁴ mol equivalent hydrogen/m²GNCC. Following this addition, CO₂ gas bubbles were observed to form andpass upwards through the suspension.

Subsequently, NaH₂PO₄.2H₂O in the form of a 30% solution is added via aperistaltic pump to the calcium carbonate suspension over a period of 10minutes in an amount corresponding to 47.8% by weight on dry calciumcarbonate weight and 3×10⁻⁴ mol H₂PO₄ anion/m² GNCC. Following thisaddition, the suspension is stirred for an additional 5 minutes.

The resulting suspension is allowed to sit overnight. The product has anSSA=72.4 m²/g and a d₅₀=7.1 μm (Malvern).

Example 5

The following Example is illustrative of the invention.

A calcium carbonate suspension is prepared by adding water and dispersedmarble (having a d₅₀ of 0.7 μm, wherein 90% of particles have a diameterof less than 2 μm) in a 20-L stainless steel reactor, such that theaqueous suspension obtained has a solids content corresponding to 16% bydry weight relative to the total suspension weight. The temperature ofthis suspension is thereafter brought to and maintained at 70° C.

Under stirring at approximately 1000 rpm such that an essentiallylaminar flow is established, acetic acid in the form a 50% solution isadded to the calcium carbonate suspension through a separation funnelover a period of 1 minute in an amount corresponding to 18.4% by weighton dry calcium carbonate weight and 3×10⁻⁴ mol equivalent hydrogen/m²GNCC. Following this addition, CO₂ gas bubbles were observed to form andpass upwards through the suspension.

Subsequently, NaH₂PO₄.2H₂O in the form of a 30% solution is added via aperistaltic pump to the calcium carbonate slurry over a period of 10minutes in an amount corresponding to 47.8% by weight on dry calciumcarbonate weight and 3×10⁻⁴ mol H₂PO₄ anion/m² GNCC. Following thisaddition, the suspension is stirred for an additional 5 minutes.

The resulting suspension is allowed to sit overnight. The product has anSSA=81.6 m²/g and a d₅₀=6.8 μm (Malvern).

Example 6

The following Example is illustrative of the invention.

A calcium carbonate suspension is prepared by adding water andundispersed chalk (having a d₅₀ of 3 μm, wherein 33% of particles have adiameter of less than 2 μm (Sedigraph)) in a 20-L stainless steelreactor, such that the aqueous suspension obtained has a solids contentcorresponding to 16% by dry weight relative to the total suspensionweight. The temperature of this suspension is thereafter brought to andmaintained at 70° C.

Under stirring at approximately 1000 rpm such that an essentiallylaminar flow is established, acetic acid in the form a 50% solution isadded to the calcium carbonate suspension through a separation funnelover a period of 1 minute in an amount corresponding to 36.8% by weighton dry calcium carbonate weight and 6×10⁻⁴ mol equivalent hydrogen/m²GNCC. Following this addition, CO₂ gas bubbles were observed to form andpass upwards through the suspension.

Subsequently, Na₂HPO₄ in the form of a 30% solution/slurry is added viaa peristaltic pump to the calcium carbonate suspension over a period of10 minutes in an amount corresponding to 43.5% by weight on calciumcarbonate weight and 3×10⁻⁴ mol HPO₄ anion/m² GNCC. Following thisaddition, the suspension is stirred for an additional 5 minutes.

The resulting suspension is allowed to sit overnight. The product has anSSA=69.6 m²/g and a d₅₀=7.5 μm (Malvern).

Example 7

The following Example is illustrative of the invention.

A calcium carbonate suspension is prepared by adding water andundispersed chalk (having a d₅₀ of 3 μm, wherein 33% of particles have adiameter of less than 2 μm (Sedigraph)) in a 20-L stainless steelreactor, such that the aqueous suspension obtained has a solids contentcorresponding to 16% by dry weight relative to the total suspensionweight. The temperature of this suspension is thereafter brought to andmaintained at 70° C.

Under stirring at approximately 1000 rpm such that an essentiallylaminar flow is established, acetic acid in the form a 50% solution isadded to the calcium carbonate suspension through a separation funnelover a period of 1 minute in an amount corresponding to 6.1% by weighton dry calcium carbonate weight and 1×10⁴ mol equivalent hydrogen/m²GNCC. Following this addition, CO₂ gas bubbles were observed to form andpass upwards through the suspension.

Subsequently, NaH₂PO₄.2H₂O in the form of a 30% solution is added via aperistaltic pump to the calcium carbonate slurry over a period of 10minutes in an amount corresponding to 15.9% by weight on calciumcarbonate weight and 1×10⁻⁴ mol H₂PO₄ anion/m² GNCC. Following thisaddition, the suspension is stirred for an additional 5 minutes.

The resulting suspension is allowed to sit overnight. The product has anSSA=33.5 m²/g and a d₅₀=6.0 μm (Malvern).

TABLE 1** Example 1 2 3 4 5 6 7 Prior art PA PA PA IN IN IN IN (PA)/invention (IN) Acid H₃PO₄ H₃PO₄ H₃PO₄ CH₃COOH CH₃COOH CH₃COOH CH₃COOHTLV <1 <1 <1 10 ppm 10 ppm 10 ppm 10 ppm Ppm ppm ppm pKa 2.12 2.12 2.124.76 4.76 4.76 4.76 Amount 3 × 10⁻⁴ 2.6 × 10⁻⁴ 9 × 10⁻⁴ 3 × 10⁻⁴ 3 ×10⁻⁴ 6 × 10⁻⁴ 1 × 10⁻⁴ acid mol mol mol mol mol mol mol added Water-none none none NaH₂PO₄ NaH₂PO₄ Na₂HPO₄ NaH₂PO₄ soluble .2H₂O .2H₂O .2H₂Osalt Amount n/a n/a n/a 3 × 10⁻⁴ 3 × 10⁻⁴ 3 × 10⁻⁴ 1 × 10⁻⁴ salt addedmol mol mol mol Total 3 × 10⁻⁴ 7.7 × 10⁻⁴ 9 × 10⁻⁴ 9 × 10⁻⁴ 9 × 10⁻⁴ 9 ×10⁻⁴ 3 × 10⁻⁴ equivalent mol mol mol mol mol mol mol H atoms added***SSA of 24.0 34.5 35.0 72.4 81.6 69.6 33.5 final product (m²/g) **allamounts acid are given in mol equivalent hydrogen/m² GNCC and allamounts salt are given in mol corresponding anion/m² GNCC ***equivalenthydrogen atoms in all of the acid and salt added to GNCC in molequivalent hydrogen/m² GNCC

1. An aqueous suspension of surface-reacted calcium carbonate obtainedby the process comprising the following steps: a) providing at least oneground natural calcium carbonate (GNCC); b) providing at least onewater-soluble acid; c) providing gaseous CO₂; d) contacting the GNCC ofstep a) with the acid of step b) and with the CO₂ of step c); wherein:(i) the at least one acid of step b) has a pK_(a) of greater than 2.5and less than or equal to 7, when measured at 20° C., and is associatedwith the ionisation of the first available hydrogen, and a correspondinganion formed on loss of the first available hydrogen that is capable offorming water-soluble calcium salts; (ii) following contacting the atleast one acid with the GNCC, at least one water-soluble salt isadditionally added, wherein the water-soluble salt is ahydrogen-containing salt having a pK_(a) of greater than 7, whenmeasured at 20° C., and is associated with the ionisation of the firstavailable hydrogen, and a salt anion is capable of formingwater-insoluble calcium salts.
 2. The aqueous suspension according toclaim 1, wherein the GNCC comprises marble, chalk, calcite, dolomite,limestone, or any mixture thereof.
 3. The aqueous suspension accordingto claim 1, wherein the pH of the aqueous suspension, measured at 20°C., is greater than 6.0.
 4. The aqueous suspension according to claim 1,wherein the pH of the aqueous suspension, measured at 20° C., is greaterthan 6.5.
 5. The aqueous suspension according to claim 1, wherein the pHof the aqueous suspension, measured at 20° C., is greater than 7.0. 6.The aqueous suspension according to claim 1, wherein the pH of theaqueous suspension, measured at 20° C., is greater than 7.5.
 7. Theaqueous suspension according to claim 1, wherein the surface-reactedcalcium carbonate has a specific surface area of more than 20 m²/g. 8.The aqueous suspension according to claim 1, wherein the surface-reactedcalcium carbonate has a specific surface area of more than 30 m²/g. 9.The aqueous suspension according to claim 1, wherein the surface-reactedcalcium carbonate has a specific surface area of more than 80 m²/g. 10.The aqueous suspension according to claim 1, wherein the surface-reactedcalcium carbonate has a specific surface area within the range of 20m²/g to 200 m²/g.
 11. The aqueous suspension according to claim 1,wherein the surface-reacted calcium carbonate has a specific surfacearea within the range of 30 m²/g to 150 m²/g.
 12. The aqueous suspensionaccording to claim 1, wherein the surface-reacted calcium carbonate hasa specific surface area within the range of 20 to 150 m²/g and a mediangrain diameter within the range of 0.1 to 50 μm.
 13. The aqueoussuspension according to claim 1, wherein the surface-reacted calciumcarbonate has a specific surface area within the range of 30 to 200 m²/gand a median grain diameter within the range of 0.1 to 50 μm.
 14. Theaqueous suspension according to claim 1, wherein the surface-reactedcalcium carbonate has a median grain diameter of from 0.1 to 50 μm. 15.The aqueous suspension according to claim 1, wherein the surface-reactedcalcium carbonate has a median grain diameter of from 1 to 25 μm. 16.The aqueous suspension according to claim 1, wherein the surface-reactedcalcium carbonate has a median grain diameter of from 3 to 15 μm. 17.The aqueous suspension according to claim 1, wherein the surface-reactedcalcium carbonate has a median grain diameter of from 5 to 12 μm. 18.The aqueous suspension according to claim 1, wherein the surface-reactedcalcium carbonate has an intra-particle porosity within the range of 20%vol to 40% vol, measured by mercury porosimetry.
 19. A solidsurface-reacted calcium carbonate obtained by drying the aqueoussuspension of claim
 1. 20. A treated surface-reacted calcium carbonateobtained by treated the solid surface-reacted calcium carbonate of claim19 with one or more fatty acids, hydrophobizing, and oleophilizingagents.
 21. Paper, tissue paper, plastic, paint, a controlled release ora water treatment agent comprising the surface-reacted calcium carbonateof the aqueous suspension of claim 1, a dried surface-reacted calciumcarbonate thereof, or dried surface-reacted calcium carbonate treatedwith one or more fatty acids, hydrophobizing, and oleophilizing agents.